THSD7A (Entrez ID: 221981)

Entrez Gene ID	221981
Official Gene Symbol	THSD7A (GeneCards)
Full name	thrombospondin type 1 domain containing 7A
Location	7p21.3
Other ids	Vega : OTTHUMG00000152346 MIM : 612249 HGNC : HGNC:22207 Ensembl : ENSG00000005108
Other names	None
Summary	The protein encoded by this gene is found almost exclusively in endothelial cells from placenta and umbilical cord. The encoded protein appears to interact with alpha(V)beta(3) integrin and paxillin to inhibit endothelial cell migration and tube formation. This protein may be involved in cytoskeletal organization. Variations in this gene may be associated with low bone mineral density in osteoporosis. [provided by RefSeq, Aug 2010]

Variants

Found 24 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
1558	221981	THSD7A	7	11485770	11485770	Autism Spectrum Disorders	NextSeq500 v2
10401	221981	THSD7A	7	11548085	11548085	Asymptomatic	NextSeq500 v2 HiSeq X Ten
10443	221981	THSD7A	7	11854995	11854995	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
10520	221981	THSD7A	7	11827564	11827564	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
10588	221981	THSD7A	7	11572254	11572254	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
10628	221981	THSD7A	7	11590036	11590036	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
10655	221981	THSD7A	7	11763597	11763597	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
10674	221981	THSD7A	7	12115525	12115525	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
11095	221981	THSD7A	7	11748246	11748246	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
11233	221981	THSD7A	7	11989647	11989647	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
11234	221981	THSD7A	7	12019870	12019870	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
11267	221981	THSD7A	7	12020491	12020491	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
11368	221981	THSD7A	7	12140450	12140450	Cockayne syndrome	NextSeq500 v2 HiSeq X Ten HiSeq 2000
11390	221981	THSD7A	7	11597917	11597917	Cockayne syndrome	NextSeq500 v2 HiSeq X Ten HiSeq 2000
11408	221981	THSD7A	7	11669176	11669176	Cockayne syndrome	NextSeq500 v2 HiSeq X Ten HiSeq 2000
11471	221981	THSD7A	7	11632300	11632300	Cockayne syndrome	NextSeq500 v2 HiSeq X Ten HiSeq 2000
11509	221981	THSD7A	7	11620988	11620988	Xeroderma Pigmentosum	NextSeq500 v2 HiSeq X Ten HiSeq 2000
11510	221981	THSD7A	7	11633903	11633903	Xeroderma Pigmentosum	NextSeq500 v2 HiSeq X Ten HiSeq 2000
26377	221981	THSD7A	7	11600330	11600330	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning
26420	221981	THSD7A	7	11625809	11625809	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning
26431	221981	THSD7A	7	11625809	11625809	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning
26472	221981	THSD7A	7	12110206	12110206	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning
29254	221981	THSD7A	7	11485770	11485770	Autism Spectrum Disorders	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning PASM
29799	221981	THSD7A	7	11485770	11485770	Autism Spectrum Disorders	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning PASM NextSeq500